Role of Hfq in Genome Evolution: Instability of G-Quadruplex Sequences in <i>E. coli</i>

• Main Authors: Virali J. Parekh, Brittany A. Niccum, Rachna Shah, Marisa A. Rivera, Mark J. Novak, Frederic Geinguenaud, Frank Wien, Véronique Arluison, Richard R. Sinden
• Format: Article
• Language: English
• Published: MDPI AG 2019-12-01
• Series: Microorganisms
• Subjects: genomic instability; quadruplex; dna; mutagenesis; nucleoid; bacterial chromatin
• Online Access: https://www.mdpi.com/2076-2607/8/1/28

Certain G-rich DNA repeats can form quadruplex in bacterial chromatin that can present blocks to DNA replication and, if not properly resolved, may lead to mutations. To understand the participation of quadruplex DNA in genomic instability in <i>Escherichia coli</i> (<i>E. coli</i>), mutation rates were measured for quadruplex-forming DNA repeats, including (G₃T)₄, (G₃T)₈, and a RET oncogene sequence, cloned as the template or nontemplate strand. We evidence that these alternative structures strongly influence mutagenesis rates. Precisely, our results suggest that G-quadruplexes form in <i>E. coli</i> cells, especially during transcription when the G-rich strand can be displaced by R-loop formation. Structure formation may then facilitate replication misalignment, presumably associated with replication fork blockage, promoting genomic instability. Furthermore, our results also evidence that the nucleoid-associated protein Hfq is involved in the genetic instability associated with these sequences. Hfq binds and stabilizes G-quadruplex structure in vitro and likely in cells. Collectively, our results thus implicate quadruplexes structures and Hfq nucleoid protein in the potential for genetic change that may drive evolution or alterations of bacterial gene expression.